ClinGen Allele Registry
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Canonical Allele Identifier:
CA12971534
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.126166744A>C
GRCh37
chr9:g.128929023A>C
Linked Data - Sequence & Population
gnomAD v2:
9:128929023 A / C
gnomAD v3:
9:126166744 A / C
gnomAD v4:
chr9-126166744-A-C
Joint Max Group AF
0.8350337 (SAS)
Genomes Max Group AF
0.8350337 (SAS)
Linked Data - NCBI & NCI
dbSNP:
888219
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.126166744A>C , CM000671.2:g.126166744A>C
GRCh38
NC_000009.11:g.128929023A>C , CM000671.1:g.128929023A>C
GRCh37
NC_000009.10:g.127968844A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'